APAC Clinical Trial Manager – Site Operations

Worldwide Clinical Trials; Australia; Remote; AUD 90,000 - 130,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research professional to lead site management activities and coordinate a team across a geographic region. You will ensure site qualification, initiation, monitoring, and close-out in alignment with study plans and SOPs.

The role requires strong leadership, regulatory knowledge, and cross-functional collaboration to deliver high-quality data and patient safety. A background in GMP/ICH and TMF management is essential.

Qualifications

• Bachelor's degree in biological/physical/health studies with 3+ years as Senior Clinical Research Associate.
• Alternative: 2-year degree with nursing or life sciences and 5+ years as Senior Clinical Research Associate.
• CTM/LCRA experience for at least 6 months acceptable; supporting main CTM and coordinating clinical operations.

Responsibilities

• Lead site management activities from study start through close-out.
• Provide leadership to the clinical site management team across monitoring activities.
• Coordinate site qualification, initiation, monitoring, and close-out visits.
• Ensure CMP adherence, TMF readiness, and quality of clinical deliverables.

Skills

Interpersonal communication

English proficiency

Planning & organization

Presentation skills

Flexibility

Multi-tasking

Negotiation & diplomacy

Problem-solving

Task prioritization

Remote team leadership

Process improvement

Customer focus

Regulatory knowledge

SOPs

Clinical operations experience

MS Office

eCRF

IVRS

IxRS

CTMS

EDC

Education

Bachelor's in biological/physical/health sciences

Nursing or life sciences degree

Tools

MS Office

eCRF

IVRS

IxRS

CTMS

EDC

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research professional to lead site management activities and coordinate a team across a geographic region. You will ensure site qualification, initiation, monitoring, and close-out in alignment with study plans and SOPs.

The role requires strong leadership, regulatory knowledge, and cross-functional collaboration to deliver high-quality data and patient safety. A background in GMP/ICH and TMF management is essential.